De Jonghe B, Cook D, Sharshar T, Lefaucheur J P, Carlet J, Outin H
Service de Réanimation Médicale, Hôpital de Poissy, France.
Intensive Care Med. 1998 Dec;24(12):1242-50. doi: 10.1007/s001340050757.
To summarize the prospective clinical studies of neuromuscular abnormalities in intensive care unit (ICU) patients. STUDY IDENTIFICATION AND SELECTION: Studies were identified through MEDLINE, EMBASE, references in primary and review articles, personal files, and contact with authors. Through duplicate independent review, we selected prospective cohort studies evaluating ICU-acquired neuromuscular disorders.
In duplicate, independently, we abstracted key data regarding design features, the population, clinical and laboratory diagnostic tests, and clinical outcomes.
We identified eight studies that enrolled 242 patients. Inception cohorts varied; some were mechanically ventilated patients for > or = 5 days, others were based on a diagnosis of sepsis, organ failure, or severe asthma while others were selected on the basis of exposure to muscle relaxants, or because of participation in muscle biochemistry studies. Weakness was systematically assessed in two of the eight studies, concerning patients with severe asthma, with a reported frequency of 36 and 70%, respectively. Electrophysiologic and histologic abnormalities consisted of both peripheral nerve and muscle involvement and were frequently reported, even in non-selected ICU patients. In a population of patients mechanically ventilated for more than 5 days, electrophysiologic abnormalities were reported in 76 % of cases. Two studies showed a clinically important increase (5 and 9 days, respectively) in duration of mechanical ventilation and a mortality twice as high in patients with critical illness neuromuscular abnormalities, compared to those without.
Prospective studies of ICU-acquired neuromuscular abnormalities include a small number of patients with various electrophysiologic findings but insufficiently reported clinical correlations. Evaluation of risk factors for these disorders and studies examining their contribution to weaning difficulties and long-term disability are needed.
总结重症监护病房(ICU)患者神经肌肉异常的前瞻性临床研究。
通过医学文献数据库(MEDLINE)、荷兰医学文摘数据库(EMBASE)、原始文章及综述文章中的参考文献、个人文档以及与作者联系来识别研究。通过重复独立评审,我们选择了评估ICU获得性神经肌肉疾病的前瞻性队列研究。
我们独立地重复提取了有关设计特征、研究人群、临床和实验室诊断测试以及临床结局的关键数据。
我们识别出八项研究,共纳入242例患者。起始队列各不相同;一些是机械通气≥5天的患者,另一些基于脓毒症、器官衰竭或重度哮喘的诊断,还有一些是根据肌肉松弛剂暴露情况选择的,或者是因为参与肌肉生物化学研究而入选。八项研究中的两项系统评估了重度哮喘患者的肌无力情况,报告的发生率分别为36%和70%。电生理和组织学异常包括周围神经和肌肉受累,即使在未经过筛选的ICU患者中也经常有报告。在机械通气超过5天的患者群体中,76%的病例报告有电生理异常。两项研究表明,与无危重症神经肌肉异常的患者相比,危重症神经肌肉异常患者的机械通气时间临床上有显著延长(分别为5天和9天),死亡率高出两倍。
关于ICU获得性神经肌肉异常的前瞻性研究纳入的患者数量较少,有各种电生理表现,但临床相关性报告不足。需要对这些疾病的危险因素进行评估,并开展研究以考察它们对脱机困难和长期残疾的影响。